FDA Adverse Event Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3020176 · Received March 25, 2013

Report

Report Number
1531186-2013-01256
Date Received
March 25, 2013
Report Date
February 26, 2013
Manufacturer
JUMAO MEDICAL EQUIPMENT
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. CUSTOMER STATES THE CASTER BROKE ON THE CHAIR. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
121442 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR JUMAO MEDICAL EQUIPMENT V18RLR

Patients

Seq Age Sex Outcome Treatment
1 Other